FAM83H Mutations Cause ADHCAI and Alter Intracellular Protein Localization

Mutations in the Beta Propeller WDR72 Cause Autosomal-Recessive Hypomaturation Amelogenesis Imperfecta

(2009) Walid El-Sayed et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Expression patterns of the Fam83h gene during murine tooth development

(2009) Min-Jung Lee et al.   ARCHIVES OF ORAL BIOLOGY

Ultrastructural Analyses of Deciduous Teeth Affected by Hypocalcified Amelogenesis Imperfecta from a Family with a Novel Y458X FAM83H Nonsense Mutation

(2009) W. El-Sayed et al.   CELLS TISSUES ORGANS

NovelFAM83Hmutations in Turkish families with autosomal dominant hypocalcified amelogenesis imperfecta

(2009)   CLINICAL GENETICS

Fam83h is Associated with Intracellular Vesicles and ADHCAI

(2009) Y. Ding et al.   JOURNAL OF DENTAL RESEARCH

Phenotypic Variation in FAM83H-associated Amelogenesis Imperfecta

(2009) J.T. Wright et al.   JOURNAL OF DENTAL RESEARCH

Competency for Nonsense-Mediated Reduction in Collagen X mRNA Is Specified by the 3′ UTR and Corresponds to the Position of Mutations in Schmid Metaphyseal Chondrodysplasia

(2008) Jacqueline T. Tan et al.   AMERICAN JOURNAL OF HUMAN GENETICS

FAM83H Mutations in Families with Autosomal-Dominant Hypocalcified Amelogenesis Imperfecta

(2008) Jung-Wook Kim et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Messenger RNA regulation: to translate or to degrade

(2008) Ann-Bin Shyu et al.   EMBO JOURNAL

Mutational spectrum ofFAM83H: the C-terminal portion is required for tooth enamel calcification

(2008) Sook-Kyung Lee et al.   HUMAN MUTATION